// Quality Doctrine

Testing
Standards

Every compound passes through a four-stage verification protocol before it leaves our facility. No exceptions, no shortcuts, no excuses.

01

HPLC Purity

High-Performance Liquid Chromatography. Every batch tested against a ≥98% purity threshold. Most lots clear 99%.

02

LC-MS Identity

Liquid chromatography-mass spectrometry confirms molecular weight and structure match specification. Zero ambiguity.

03

Endotoxin Screening

LAL bacterial endotoxin testing on every handling-grade lot. Documented and lot-coded.

04

Cold-Chain Verified

Temperature-logged shipping with insulated packaging and dry-ice options for thermally sensitive compounds.

// Protocol

Lot-to-Door Chain of Custody

Step 01

Synthesis

Sourced from cGMP-aligned partners with documented synthesis protocols.

Step 02

Verification

Independent US lab analysis. COA generated and lot-coded.

Step 03

Vault

Climate-controlled storage in our Las Vegas facility. Inventory under camera.

Step 04

Dispatch

Insulated, discreet packaging. Tracking activated within 12 hours.

Certificate of Analysis

Every shipment includes a lot-specific Certificate of Analysis detailing purity, identity, and test methodology. COAs are archived for a minimum of 36 months and available on request.

COA · SAMPLELOT-SCP-2025-001
Compound
BPC-157
Method
HPLC-UV @ 220nm
Purity
99.41%
Mass Spec
Confirmed
Endotoxin
< 0.5 EU/mg
Appearance
White lyophilized powder
Released
2025-04-12
For Research Use Only